Canonical Allele Identifier: CA2224380096

Gene: HERPUD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56935168T= , CM000678.2:g.56935168T=	GRCh38
NC_000016.9:g.56969080T= , CM000678.1:g.56969080T=	GRCh37
NC_000016.8:g.55526581T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439977.7:c.148-67T= MANE Select	ENSP00000409555.2:n.148-67T=
ENST00000300302.9:c.148-67T=	ENSP00000300302.5:n.148-67T=
ENST00000344114.8:c.148-67T=	ENSP00000340931.4:n.148-67T=
ENST00000379792.6:c.148-67T=	ENSP00000369118.2:n.148-67T=
ENST00000439977.6:c.148-67T=	ENSP00000409555.2:n.148-67T=
ENST00000562914.1:n.251-67T=
ENST00000563343.5:c.22-67T=	ENSP00000455094.1:n.22-67T=
ENST00000565966.5:c.148-74T=	ENSP00000456384.1:n.148-74T=
ENST00000566550.1:n.204T=
ENST00000568676.5:n.246-67T=
ENST00000569429.5:c.22-67T=	ENSP00000457321.1:n.22-67T=
ENST00000569569.5:n.246-67T=
ENST00000570273.5:n.245-67T=
NM_001010989.2:c.148-67T=	NP_001010989.1:n.148-67T=
NM_001272103.1:c.148-67T=	NP_001259032.1:n.148-67T=
NM_014685.3:c.148-67T=	NP_055500.1:n.148-67T=
XM_006721352.2:c.331-67T=	XP_006721415.1:n.331-67T=
NM_014685.4:c.148-67T= MANE Select	NP_055500.1:n.148-67T=
NM_001010989.3:c.148-67T=	NP_001010989.1:n.148-67T=
NM_001272103.2:c.148-67T=	NP_001259032.1:n.148-67T=